U. Gruber-Sedlmayr

Rare variants in γ‐aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes

A. Hofman, A. Uitterlinden, C. V. van Duijn, 2015, Annals of neurology.

Epileptic phenotypes, electroclinical features and clinical characteristics in 17 children with anti-NMDAR encephalitis.

M. Ensslen, K. Rostásy, I. Borggraefe, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The burden of pneumococcal meningitis in Austrian children between 2001 and 2008

D. Klobassa, K. Pfurtscheller, A. Vécsei, 2014, European Journal of Pediatrics.

Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy

P. May, R. Krause, R. Balling, 2018, European Journal of Human Genetics.

Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation

W. Schmidt, B. Plecko, M. Lee-Kirsch, 2017, Pediatric Rheumatology.

Prognostic relevance of MOG antibodies in children with an acquired demyelinating syndrome

K. Rostásy, A. Blaschek, B. Anlar, 2017, Neurology.